Canonical Allele Identifier: CA8001221

Gene: ALDOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30070046G>T , CM000678.2:g.30070046G>T	GRCh38
NC_000016.9:g.30081367G>T , CM000678.1:g.30081367G>T	GRCh37
NC_000016.8:g.29988868G>T	NCBI36
NG_008010.1:g.21877G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338110.11:c.*1508+17G>T	ENSP00000336927.6:n.*1508+17G>T
ENST00000338110.10:c.*1508+17G>T	ENSP00000336927.6:n.*1508+17G>T
ENST00000395248.6:c.*1181+17G>T	ENSP00000378669.2:n.*1181+17G>T
ENST00000566897.6:c.*1508+17G>T	ENSP00000455724.2:n.*1508+17G>T
ENST00000642816.3:c.1161+17G>T MANE Select	ENSP00000496166.1:n.1161+17G>T
ENST00000643777.4:c.999+17G>T	ENSP00000494188.2:n.999+17G>T
ENST00000338110.9:c.999+17G>T	ENSP00000336927.5:n.999+17G>T
ENST00000395240.7:c.1011+17G>T	ENSP00000378661.3:n.1011+17G>T
ENST00000395248.5:c.1161+17G>T	ENSP00000378669.1:n.1161+17G>T
ENST00000412304.6:c.999+17G>T	ENSP00000400452.2:n.999+17G>T
ENST00000563060.6:c.999+17G>T	ENSP00000455800.2:n.999+17G>T
ENST00000564521.6:n.2193+17G>T
ENST00000564546.5:c.999+17G>T	ENSP00000455917.1:n.999+17G>T
ENST00000564595.6:c.1161+17G>T	ENSP00000457468.2:n.1161+17G>T
ENST00000565355.1:c.296+17G>T
ENST00000566130.1:n.503+17G>T
ENST00000566897.5:c.999+17G>T	ENSP00000455724.1:n.999+17G>T
ENST00000569545.5:c.999+17G>T	ENSP00000455700.1:n.999+17G>T
ENST00000569798.5:c.1016G>T	ENSP00000455857.1:p.Arg339Met
ENST00000627059.2:c.1011+17G>T	ENSP00000485952.1:n.1011+17G>T
NM_000034.3:c.999+17G>T	NP_000025.1:n.999+17G>T
NM_001127617.2:c.999+17G>T	NP_001121089.1:n.999+17G>T
NM_001243177.1:c.1161+17G>T	NP_001230106.1:n.1161+17G>T
NM_184041.2:c.999+17G>T	NP_908930.1:n.999+17G>T
NM_184043.2:c.999+17G>T	NP_908932.1:n.999+17G>T
XM_011545767.1:c.999+17G>T	XP_011544069.1:n.999+17G>T
XM_011545768.1:c.999+17G>T	XP_011544070.1:n.999+17G>T
NM_001243177.2:c.1161+17G>T	NP_001230106.1:n.1161+17G>T
NM_001365304.1:c.*1508+17G>T	NP_001352233.1:n.*1508+17G>T
NM_001365305.1:c.*1508+17G>T	NP_001352234.1:n.*1508+17G>T
NM_001365307.1:c.*1508+17G>T	NP_001352236.1:n.*1508+17G>T
NM_184041.3:c.999+17G>T	NP_908930.1:n.999+17G>T
XM_024450192.1:c.999+17G>T	XP_024305960.1:n.999+17G>T
XM_024450193.1:c.999+17G>T	XP_024305961.1:n.999+17G>T
NM_001243177.3:c.1161+17G>T	NP_001230106.1:n.1161+17G>T
NM_001365307.2:c.*1508+17G>T	NP_001352236.1:n.*1508+17G>T
NM_184041.4:c.999+17G>T	NP_908930.1:n.999+17G>T
NM_001243177.4:c.1161+17G>T MANE Select	NP_001230106.1:n.1161+17G>T
NM_001365304.2:c.*1508+17G>T	NP_001352233.1:n.*1508+17G>T
NM_001365305.2:c.*1508+17G>T	NP_001352234.1:n.*1508+17G>T
NM_184041.5:c.999+17G>T	NP_908930.1:n.999+17G>T